839674-89-4

Basic information

• Product Name: 2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[2-(2-phenyl-1,3-dioxan-5-ylidene)ethyl]-
• CAS NO: 839674-89-4
• Molecular Formula: C17H18N2O4
• Molecular Weight: 314.341
• Mol File: 839674-89-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[2-(2-phenyl-1,3-dioxan-5-ylidene)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[2-(2-phenyl-1,3-dioxan-5-ylidene)ethyl]-(839674-89-4)
• EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 5-methyl-1-[2-(2-phenyl-1,3-dioxan-5-ylidene)ethyl]-(839674-89-4)

Safety Data

• Hazardous Substances Data: 839674-89-4(Hazardous Substances Data)

Upstream product

• 65-71-4 thymin 
• 3290-74-2 5-methylene-2-phenyl-[1,3]dioxolane 
• 70184-00-8 1-allyl-5-methyl-1H-pyrimidine-2,4-dione 

Relevant articles and documents

Efficient synthesis of various acycloalkenyl derivatives of pyrimidine using cross-metathesis and Pd(0) methodologies

Novel acyclonucleosides (9a-d, 10a-d, 18a,b and 19a,b) have been prepared using Pd(0) and cross-metathesis methodologies. The allylic N-alkylation under Tsuji-Trost conditions was used to introduce the nucleobase, while the Suzuki-Miyaura reaction afforded C-5 substituted uracil analogues. The cross-metathesis performed with a ruthenium catalyst was used to provide new acycloalkenyl nucleosides. The antiviral activities of all final compounds have been evaluated. Novel acyclonucleosides (9a-d, 10a-d, 18a,b and 19a,b) were prepared using Pd(0) and cross-metathesis methodologies. The allylic N-alkylation under Tsuji-Trost conditions was used to introduce the nucleobase, meanwhile the Suzuki-Miyaura reaction afforded C-5 substituted uracil analogues. A ruthenium-based cross-metathesis reaction was used to synthesize new acycloalkenyl nucleosides.